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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT01205191 |
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Date of registration:
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16/09/2010 |
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Primary sponsor: |
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Public title:
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Cell Phone-supported Cognitive Behavioural Therapy
LINNEA |
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Scientific title:
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Effectiveness Study of Cell Phone-supported Cognitive Behavioural Therapy for Anxiety Disorders in Frontline Settings |
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Date of first enrolment:
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April 2011 |
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Target sample size:
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400 |
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Recruitment status: |
Recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT01205191 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research
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Countries of recruitment
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Sweden
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Contacts
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Name:
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Karin Halje, MSc |
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Address:
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Telephone:
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+46 10 103 0000 |
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Email:
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karin.halje.lindgren@lio.se |
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Affiliation:
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Name:
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Toomas Timpka, MD PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Section of Social Medicine/LiU |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- age 18 to 25; and
- scoring 7 or higher on the anxiety section of the Hospital Anxiety and Depression
scale (HADS) at initial evaluation.
Exclusion Criteria:
- at the initial evaluation displays symptoms indicative for referral to a psychiatric
specialist, e.g. active suicidal ideas or symptoms of a psychotic disorder, organic
mental disorder or alcohol and/or drug dependence; or
- is unable to read, write or speak in the Swedish;
Age minimum:
18 Years
Age maximum:
25 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Anxiety
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Intervention(s)
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Behavioral: CBT
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Behavioral: CBT with digital audio player support
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Behavioral: Cell-phone supported CBT
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Primary Outcome(s)
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Anxiety
[Time Frame: Six months after treatment]
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Secondary Outcome(s)
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Adherence
[Time Frame: 14 weeks]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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